Pharmaceutical industry
Your GMP compliance rests on critical actions. Secure them.
In pharmaceutical production, GMP compliance plays out at the workstation: on an intervention in a sterile area, a weighing, a batch-record review, a deviation handling. This critical know-how stays largely informal, in the heads of your experienced operators, your QA and your QC. Sinfony captures it so that mastery — and data integrity — no longer depend on key people.
The problem
Validated doesn't mean mastered.
Your SOPs are approved, your training records signed off. But between the procedure and the real action in sterile production, the gap remains — and it fuels deviations, recurring CAPAs and inspection observations. Data integrity, asepsis and batch release demand a consistent execution that documentation alone cannot guarantee.
100%
of staff must be trained for their activities: a GMP requirement, not an option.
80%
of critical know-how stays informal, held by a few operators and QA/QC experts.
Deviations & CAPA
Cut recurring deviations by tackling the root cause: the poorly transmitted action.
Data integrity
Embed the right ALCOA+ reflexes into daily practice at the workstation.
Sterile production
Secure aseptic interventions through the filmed, standardized action.
Our solutions
Capture GMP know-how, for the long run.
Three complementary levers, from ready-to-use content to field consulting.
Academy
Ready-to-deploy GMP and pharma-quality modules: data integrity, deviations, QA/QC, in-area hygiene.
Explore the catalog → PlatformLearning Suite
Auditable certificates and audit-ready traceability to prove every operator's qualification.
See the platform → ConsultingConsulting
Field assessment, deviation reduction and SOP simplification, with the method transferred to your teams. From €5k.
Request an assessment →Our results
The proof, in numbers.
What pharmaceutical sites see once their critical actions are captured.
- −15 to −30%
- deviations
- −50%
- deviation handling time
- −95%
- training-related errors
- 20,000
- certificates that stand up to inspectors
"You're the consultants with the nerve to actually make things move."
Training
Academy paths for this sector.
Discover our solutions for your sector.
Sinfony, the Académie de la Qualité Efficace and Bio15Pharma work together — each on its own trade, with no overlap.
With the Académie de la Qualité Efficace
Deviations, CAPA, release
Investigations that change something. We clear the backlog, then what produced it — in that order, never the reverse.
With Bio15Pharma
An expert on site within 5 days
A critical post left vacant, an inspection round the corner: the expert is identified within 24 hours and on your site within 5 days.
Sinfony × AQE × Bio15Pharma
Integrated quality support
Procedures, training, release flow, shop floor: when the need spans more than one subject, the three houses work together.
Request an assessment.
A Sinfony expert reviews your deviations, your SOPs and your critical GMP actions with your teams.